%0 Journal Article %1 Kramer1992 %A Kramer, M. R. %A Stoehr, C. %A Lewiston, N. J. %A Starnes, V. A. %A Theodore, J. %D 1992 %J Transplantation %K antifolates transplantation pneumonia prophylaxis %N 3 %P 586--589 %T Trimethoprim-sulfamethoxazole prophylaxis for Pneumocystis carinii infections in heart-lung and lung transplantation--how effective and for how long? %V 53 %X Pneumocystis carinii pneumonia (PCP) is a common clinical problem in the setting of organ transplantation, particularly in heart-lung and lung allograft recipients. Without prophylactic measurements, the incidence of P carinii pneumonia can reach up to 88\% of heart-lung transplant recipients. We conducted a retrospective analysis of the Stanford heart-lung and lung transplant experience in order to assess the efficacy of the prophylactic therapy and to try to define the duration of therapy necessary for prevention. During a 9-year period 82 heart-lung and 13 single-lung transplants were performed. Of the patients not on prophylaxis therapy 27\% (13 patients) developed P carinii infection as compared with 0\% of patients on trimethoprim-sulfamethoxazole (TMP-SMX) prophylaxis. The incidence of PCP infection peaked between 3 and 6 months posttransplantation. No case of infection was observed before the 7th week posttransplant. PCP was more common following induction immunosuppression with OKT3 as compared with RATG (P less than 0.05). All cases of infections later than one year posttransplant were associated with recent increase in the immunosuppression regimen with high-dose corticosteroids for treatment of acute or chronic (obliterative bronchiolitis) rejection. Although our study is retrospective and based on various immunosuppressive and diagnostic technique periods, it seems that TMP-SMX is highly effective in preventing PCP infections in heart-lung and lung transplant recipients. Twelve months of therapy is probably a sufficient length of therapy if immunosuppressive therapy is stable. However, whenever augmentation in the immunosuppression regimen is indicated, prophylactic therapy should promptly be restarted.

@article{Kramer1992, abstract = {Pneumocystis carinii pneumonia (PCP) is a common clinical problem in the setting of organ transplantation, particularly in heart-lung and lung allograft recipients. Without prophylactic measurements, the incidence of P carinii pneumonia can reach up to 88\% of heart-lung transplant recipients. We conducted a retrospective analysis of the Stanford heart-lung and lung transplant experience in order to assess the efficacy of the prophylactic therapy and to try to define the duration of therapy necessary for prevention. During a 9-year period 82 heart-lung and 13 single-lung transplants were performed. Of the patients not on prophylaxis therapy 27\% (13 patients) developed P carinii infection as compared with 0\% of patients on trimethoprim-sulfamethoxazole (TMP-SMX) prophylaxis. The incidence of PCP infection peaked between 3 and 6 months posttransplantation. No case of infection was observed before the 7th week posttransplant. PCP was more common following induction immunosuppression with OKT3 as compared with RATG (P less than 0.05). All cases of infections later than one year posttransplant were associated with recent increase in the immunosuppression regimen with high-dose corticosteroids for treatment of acute or chronic (obliterative bronchiolitis) rejection. Although our study is retrospective and based on various immunosuppressive and diagnostic technique periods, it seems that TMP-SMX is highly effective in preventing PCP infections in heart-lung and lung transplant recipients. Twelve months of therapy is probably a sufficient length of therapy if immunosuppressive therapy is stable. However, whenever augmentation in the immunosuppression regimen is indicated, prophylactic therapy should promptly be restarted.}, added-at = {2012-06-16T03:51:47.000+0200}, author = {Kramer, M. R. and Stoehr, C. and Lewiston, N. J. and Starnes, V. A. and Theodore, J.}, biburl = {https://www.bibsonomy.org/bibtex/20c8040355a7cd20d5cd955f3b0637257/aorchid}, description = {Retrospective single study mixed cohort. Basically 26% of those not on prophy got disease, while none on prophy did. Median time 117d, none prior to 59 days. After increase in steroid saw more between days 15 and 90; this is where late disease came from.}, file = {bactrim prophy in lung transplant:ID_General/TransplantClinical/Transplantation.53.586.pdf:PDF}, groups = {public}, institution = {Department of Medicine, Stanford University School of Medicine, California 94305.}, interhash = {f50772824ad2122469913e83df03ddf7}, intrahash = {0c8040355a7cd20d5cd955f3b0637257}, journal = {Transplantation}, keywords = {antifolates transplantation pneumonia prophylaxis}, language = {eng}, medline-pst = {ppublish}, month = Mar, number = 3, pages = {586--589}, pmid = {1549851}, timestamp = {2012-06-16T03:51:47.000+0200}, title = {Trimethoprim-sulfamethoxazole prophylaxis for Pneumocystis carinii infections in heart-lung and lung transplantation--how effective and for how long?}, username = {aorchid}, volume = 53, year = 1992 }